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Page 1
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects.
Simon AJ, Lev A, Zhang Y, Weiss B, Rylova A, Eyal E, Kol N, Barel O, Cesarkas K, Soudack M, Greenberg-Kushnir N, Rhodes M, Wiest DL, Schiby G, Barshack I, Katz S, Pras E, Poran H, Reznik-Wolf H, Ribakovsky E, Simon C, Hazou W, Sidi Y, Lahad A, Katzir H, Sagie S, Aqeilan HA, Glousker G, Amariglio N, Tzfati Y, Selig S, Rechavi G, Somech R. Simon AJ, et al. Among authors: simon c. J Exp Med. 2016 Jul 25;213(8):1429-40. doi: 10.1084/jem.20151618. Epub 2016 Jul 18. J Exp Med. 2016. PMID: 27432940 Free PMC article.
Nuclear envelopathies--raising the nuclear veil.
Somech R, Shaklai S, Amariglio N, Rechavi G, Simon AJ. Somech R, et al. Among authors: simon aj. Pediatr Res. 2005 May;57(5 Pt 2):8R-15R. doi: 10.1203/01.PDR.0000159566.54287.6C. Epub 2005 Apr 6. Pediatr Res. 2005. PMID: 15817509 Review.
Gene silencing at the nuclear periphery.
Shaklai S, Amariglio N, Rechavi G, Simon AJ. Shaklai S, et al. Among authors: simon aj. FEBS J. 2007 Mar;274(6):1383-92. doi: 10.1111/j.1742-4658.2007.05697.x. FEBS J. 2007. PMID: 17489096 Free article. Review.
A LAD-III syndrome is associated with defective expression of the Rap-1 activator CalDAG-GEFI in lymphocytes, neutrophils, and platelets.
Pasvolsky R, Feigelson SW, Kilic SS, Simon AJ, Tal-Lapidot G, Grabovsky V, Crittenden JR, Amariglio N, Safran M, Graybiel AM, Rechavi G, Ben-Dor S, Etzioni A, Alon R. Pasvolsky R, et al. Among authors: simon aj. J Exp Med. 2007 Jul 9;204(7):1571-82. doi: 10.1084/jem.20070058. Epub 2007 Jun 18. J Exp Med. 2007. PMID: 17576779 Free PMC article.
243 results